HSP27 and HSP70 Potentially Oncogenic Apoptosis Inhibitors

被引:211
作者
Garrido, Carmen [1 ]
Schmitt, Elise [1 ]
Cande, Celine [2 ]
Vahsen, Nicola [2 ]
Parcellier, Arnaud [1 ]
Kroemer, Guido [2 ]
机构
[1] Fac Med & Pharm Dijon, INSERM, U517, Dijon, France
[2] Inst Gustave Roussy, CNRS, UMR 8135, Pavillon Rech 1,39 Rue Camille Desmoulins, F-94805 Villejuif, France
关键词
heat shock proteins; cancer cell growth; apoptosis inducing factor; cytochrome c; cancer cell resistance;
D O I
10.4161/cc.2.6.521
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Stress or heat shock proteins (HSPs) such as HSP27 and HSP70 are expressed in response to a wide variety of physiological and environmental insults including heat, reactive oxygen species or anticancer drugs. Their overexpression allows cells to survive to otherwise lethal conditions. Several different mechanisms may account for the cyto-protective activity of HSP27 and HSP70. First, both proteins are powerful chaperones. Second, both inhibit key effectors of the apoptotic machinery including the apoptosome, the caspase activation complex (both HSP27 and HSP70), and apoptosis inducing factor (only HSP70). Third, they both play a role in the proteasome-mediated degradation of apoptosis-regulatory proteins. HSP27 and HSP70 may participate in oncogenesis, as suggested by the fact that overexpression of heat shock proteins can increase the tumorigenic potential of tumor cells. The down-regulation or selective inhibition of HSP70 might constitute a valuable strategy for the treatment of cancer.
引用
收藏
页码:579 / 584
页数:6
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